By Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant Science
Intervening time file of the Institute of Medicine's Committee on Transmissible Spongiform Encephalopathies: review of appropriate technological know-how, convened to supply suggestion to the U.S. division of safeguard concerning prion disorder. specializes in the study had to increase diagnostics for prion ailments and discusses prion learn infrastructure concerns. Softcover.
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1991. ” Current Topics in Microbiology and Immunology 172:195-232. Scott MR, Will R, Ironside J, Nguyen HO, Tremblay P, DeArmond SJ, Prusiner SB. 1999. Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans. Proceedings of the National Academy of Sciences of the United States of America 96(26):15137-15142. Telling GC, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen FE, DeArmond SJ, Prusiner SB. 1995. Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein.
Harvard Center for Risk Analysis, Harvard School of Public Health, Center for Computational Epidemiology, College of Veterinary Medicine, Tuskegee University. 2001. Executive summary. Evaluation of the Potential for BSE in the United States. S. Department of Agriculture. Haywood AM. 1997. Transmissible spongiform encephalopathies. New England Journal of Medicine 337(25):1821-1828. Huillard d'Aignaux JN, Cousens SN, Maccario J, Costagliola D, Alpers MP, Smith PG, Alperovitch A. 2002. The incubation period of kuru.
Clinically, this destruction manifests itself differently in different species, but inevitably, it seems to lead to death. Both the incubation period and the length of time between the onset of clinical symptoms and death vary widely depending on the host species and the strain of PrPSc. Investigators initially differentiated among prion strains through clinical observations of goats that displayed either drowsy or hyperactive behaviors (Pattison and Millson, 1961). Later work with mice revealed that genetic factors play a role in determining strain differences.
Advancing Prion Science by Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant Science